Evidence map›Paper›PMID 35078814›Full record

ArticleCancer research2022

Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma.

Julie Devin, Tatiana Cañeque, Yea-Lih Lin, Lucie Mondoulet, Jean-Luc Veyrune, Matthieu Abouladze, Elvira Garcia De Paco, Ouissem Karmous Gadacha, Guillaume Cartron, Philippe Pasero and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.3field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 31 citations in OpenAlex.

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  18. Targeting iron to contrast cancer progression.Current opinion in chemical biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Julie DevinDepartment of Biological Hematology, CHU Montpellier, Montpellier, France.ORCID 0000-0001-8929-6992
Tatiana CañequeChemical Biology of Cancer Laboratory, Institut Curie, 26 rue d'Ulm, 75248 Paris Cedex 05, France; PSL Université, Paris, France; CNRS UMR 3666, Paris, France; INSERM U1143, Paris, France.ORCID 0000-0002-1110-0643
Yea-Lih LinInstitute of Human Genetics, UMR 9002 CNRS-UM, Montpellier, France.ORCID 0000-0003-4063-0771
Lucie MondouletSideRos, Paris, France.ORCID 0000-0003-0110-0321
Jean-Luc VeyruneInstitute of Human Genetics, UMR 9002 CNRS-UM, Montpellier, France.
Matthieu AbouladzeDepartment of Biological Hematology, CHU Montpellier, Montpellier, France.
Elvira Garcia De PacoDepartment of Biological Hematology, CHU Montpellier, Montpellier, France.
Ouissem Karmous GadachaDepartment of Biological Hematology, CHU Montpellier, Montpellier, France.
Guillaume CartronClinical Hematology, CHU Montpellier, Montpellier, France.ORCID 0000-0003-0659-9635
Philippe PaseroInstitute of Human Genetics, UMR 9002 CNRS-UM, Montpellier, France.ORCID 0000-0001-5891-0822
Caroline BretDepartment of Biological Hematology, CHU Montpellier, Montpellier, France.
Raphaël RodriguezChemical Biology of Cancer Laboratory, Institut Curie, 26 rue d'Ulm, 75248 Paris Cedex 05, France; PSL Université, Paris, France; CNRS UMR 3666, Paris, France; INSERM U1143, Paris, France.ORCID 0000-0001-7668-446X
Jerome MoreauxDepartment of Biological Hematology, CHU Montpellier, Montpellier, France.ORCID 0000-0002-5717-3207
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Montpellier · FRDélégation Paris 7 · FRUniversité de Montpellier · FR

Funding

European Research Council 647973
6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common hematological malignancy. Although more than half of patients with DLBCL achieve long-term remission, the majority of remaining patients succumb to the disease. As abnormal iron homeostasis is implicated in carcinogenesis and the progression of many tumors, we searched for alterations in iron metabolism in DLBCL that could be exploited to develop novel therapeutic strategies. Analysis of the iron metabolism gene expression profile of large cohorts of patients with DLBCL established the iron score (IS), a gene expression-based risk score enabling identification of patients with DLBCL with a poor outcome who might benefit from a suitable targeted therapy. In a panel of 16 DLBCL cell lines, ironomycin, a promising lysosomal iron-targeting small molecule, inhibited DLBCL cell proliferation at nanomolar concentrations compared with typical iron chelators. Ironomycin also induced significant cell growth inhibition, ferroptosis, and autophagy. Ironomycin treatment resulted in accumulation of DNA double-strand breaks, delayed progression of replication forks, and increased RPA2 phosphorylation, a marker of replication stress. Ironomycin significantly reduced the median number of viable primary DLBCL cells of patients without major toxicity for nontumor cells from the microenvironment and presented low toxicity in hematopoietic progenitors compared with conventional treatments. Significant synergistic effects were also observed by combining ironomycin with doxorubicin, BH3 mimetics, BTK inhibitors, or Syk inhibitors. Altogether, these data demonstrate that a subgroup of high-risk patients with DLBCL can be identified with the IS that can potentially benefit from targeting iron homeostasis. SIGNIFICANCE: Iron homeostasis represents a potential therapeutic target for high-risk patients with DLBCL that can be targeted with ironomycin to induce cell death and to sensitize tumor cells to conventional treatments.

Indexed as

ApoptosisLymphoma, Large B-Cell, DiffuseCell Line, TumorCell ProliferationHomeostasisHumansIronTumor MicroenvironmentIron

Identifiers

PMID35078814
PMCPMC9359736
OpenAlexW4207082851

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.